Workshops on ISO 14971
Quality and Risk Management are crucial to success in the competitive medical device industry. Internal quality audits allow organizations to assess their own Quality Management system, which is the basis for regulatory compliance, and to show committment to meeting customers’ requirements. It also ensure that the framework remains effective.
Risk Management concepts are also important to stakeholders including medical practitioners, health care service providers, governments, industry, patients and the general public. A systematic process to identify hazards in medical devices, and to monitor effectiveness of control measures, helps in the risk management of medical devices during its product lifecycle.
Through these workshops, participants will have an overview of ISO 14971 requirements, gain auditing skills through a mix of tutorials, role-play, group workshops and open forum discussions. Participants will also get to understand the implementation of risk management throughout the life-cycle of a medical device.
Seminar Details | |
Date | 8th October Workshop on Risk Management of Medical Devices according to EN ISO 14971:2012 |
Time | 9.00 am - 5.00 pm |
Venue | |
Fees | a) Early bird discount fee The following training fee of applies if registration and payment are received latest by 7th September 2015:
b) Normal registration fee The following training fee of applies if registration and/or payment is received after 7th September 2015:
c) Group discount fee 10% discount off total training fee (before 7% GST) applies when at least 3 participants from the same organization registered by 7th September 2015. |
Please refer to the outline for more information. [ PDF 492 kB ]
To reserve a space, please submit your details using the online form as below. You may also contact:
Mr. Caleb Ng - Tel: +65 6885 1475 / Email:caleb.ng@tuv-sud-psb.sg
Ms Bernice Lau - Tel: +65 6885 1645 / Email: bernice.lau@tuv-sud-psb.sg
Thank you very much, and we look forward to your participation.